510(k) · Cleared
ClearedColonglide (R) Lubricant
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Pediatric Pharmaceuticals, Inc. · KMJ Lubricant, Patient
Cleared on Oct 3, 2013 as substantially equivalent to K974768 (Nice-Pak Products, Inc., 1998) and 1 other predicate after a 122-day review. Its family tree reaches back 1 generation to 1995.
- Decided
- Oct 3, 2013
- Review
- 122 days
- Class
- Class I
- Product code
- KMJ
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 1 generation to K951431 (1995). 2 ancestors in all. No later device cites it as a predicate yet.
- Root · 1 generation backK951431 Aquagel Lubricating JellyDepuy Healthcare · 1995
- This deviceK131617 Colonglide (R) LubricantPediatric Pharmaceuticals, Inc. · 2013
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K951431 | Aquagel Lubricating Jelly | Depuy Healthcare | 1995 | — |
| 0 (this device) | K131617 | Colonglide (R) Lubricant | Pediatric Pharmaceuticals, Inc. | 2013 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1998 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in KMJ? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the report
What was it cleared against? (2)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K974768 | Pdi Sterile Lubricating JellySummary page 1…ssification Panel: General Hospital Panel Product Code: KMJ 3. Predicate Device PD!® Sterile Lubricating Jelly (Nice-Pack Products Inc., K974768) Aquagelo Lubricating Jelly (DePuy Healthcare, K95 143 1) 4. Device Description Colonglide®o Lubricant is a clear, colorle… | 1998 |
| * | K951431 | Aquagel Lubricating JellySummary page 1…uct Code: KMJ 3. Predicate Device PD!® Sterile Lubricating Jelly (Nice-Pack Products Inc., K974768) Aquagelo Lubricating Jelly (DePuy Healthcare, K95 143 1) 4. Device Description Colonglide®o Lubricant is a clear, colorless, non-sterile, odorless, water-based patient lubricant.… | 1995 |
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- None of the 2 ancestors has a recall.
- 1 other device also cites its predicate K974768.
How does its category compare?
All KMJ devicesKMJ Lubricant, Patient: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.
FDA decisions per year · KMJ
1in 2015
2026 to Oct 25, outlined.
Median 510(k) review, days · KMJ
141in 2012
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · KMJ
1in 2016
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · KMJ
1in 2025
MAUDE reports naming product code KMJ, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 5 |
| 2008 | 3 | 86 | 0 | 3 |
| 2009 | 1 | — | 0 | 1 |
| 2010 | 1 | — | 1 | 1 |
| 2011 | 1 | — | 12 | 7 |
| 2012 | 3 | 141 | 0 | 2 |
| 2013 | 1 | — | 0 | 6 |
| 2014 | 1 | — | 0 | 2 |
| 2015 | 1 | — | 0 | 4 |
| 2016 | 0 | — | 1 | 5 |
| 2017 | 0 | — | 0 | 1 |
| 2018 | 0 | — | 0 | 5 |
| 2019 | 0 | — | 0 | 2 |
| 2020 | 0 | — | 0 | 1 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 4 |
| 2023 | 0 | — | 0 | 4 |
| 2024 | 0 | — | 0 | 3 |
| 2025 | 0 | — | 0 | 1 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The Colonglideo Lubricant Isindicated for medical purposes for use to lubricate a body orifice of a patient in order to facilitate the entry of a diagnostic or therapeutic medical device (such as an endloscope). This device is Intended for use on order of a physician.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K131617 · printed Nov 6, 2026
Cite this page
510(k) Report. “K131617: Colonglide (R) Lubricant.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K131617
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026